510(k) K133103 ยท MNI Orthosis, Spinal Pedicle Fixation
AVERSION PEDICLE SCREW SYSTEM
| Applicant | K7, LLC, Chesterland OH, US |
| Decision | Substantially Equivalent, Jan 27, 2014 |
| Received | Sep 30, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K133103
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.